猪早期卵发生的时空动态

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Wei Ge, Yi-Lin Niu, Yu-Kang Li, Li Li, Han Wang, Wen-Wen Li, Tian Qiao, Yan-Ni Feng, Yu-Qing Feng, Jing Liu, Jun-Jie Wang, Xiao-Feng Sun, Shun-Feng Cheng, Lan Li, Wei Shen
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引用次数: 0

摘要

在人类和其他哺乳动物中,卵子发生过程在卵巢特定区域异步启动,导致休眠卵泡和生长卵泡分别定位于皮质和髓质;然而,目前对这一过程的了解仍然不足。在此,我们整合了单细胞RNA测序(scRNA-seq)和空间转录组学(ST)来了解基因的时空表达谱,并探索猪卵子发生早期卵巢微环境的空间组织。将不同阶段的生殖细胞群投射到空间图谱中,揭示了发育中的猪卵巢中生殖细胞的“皮层到髓质(C-M)”分布。猪和人类之间的跨物种分析揭示了生殖细胞在卵子发生过程中保守的C-M分布模式,突出了猪作为在空间背景下研究人类卵子发生的有价值模型的实用性。利用ST进行RNA速度分析,鉴定了猪卵巢皮层和髓质区颗粒细胞系的分子特征和空间动力学。空间共现分析和细胞间通讯分析揭示了生殖细胞和体细胞在皮层和髓质区域的独特的细胞间通讯模式。值得注意的是,卵巢组织的体外培养证实了细胞间NOTCH信号和细胞外基质(ECM)蛋白在启动减数分裂和卵子生成程序中起着至关重要的作用,突出了卵巢微环境在协调生殖细胞命运中的作用。总的来说,我们的工作提供了对早期卵子发生的空间特征和卵巢微环境在空间背景下对生殖细胞命运的调节作用的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatiotemporal dynamics of early oogenesis in pigs
In humans and other mammals, the process of oogenesis initiates asynchronously in specific ovarian regions, leading to the localization of dormant and growing follicles in the cortex and medulla, respectively; however, the current understanding of this process remains insufficient. Here, we integrate single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics (ST) to comprehend spatial–temporal gene expression profiles and explore the spatial organization of ovarian microenvironments during early oogenesis in pigs. Projection of the germ cell clusters at different stages of oogenesis into the spatial atlas unveils a “cortical to medullary (C-M)” distribution of germ cells in the developing porcine ovaries. Cross-species analysis between pigs and humans unveils a conserved C-M distribution pattern of germ cells during oogenesis, highlighting the utility of pigs as valuable models for studying human oogenesis in a spatial context. RNA velocity analysis with ST identifies the molecular characteristics and spatial dynamics of granulosa cell lineages originating from the cortical and medullary regions in pig ovaries. Spatial co-occurrence analysis and intercellular communication analysis unveils a distinct cell–cell communication pattern between germ cells and somatic cells in the cortex and medulla regions. Notably, in vitro culture of ovarian tissues verifies that intercellular NOTCH signaling and extracellular matrix (ECM) proteins played crucial roles in initiating meiotic and oogenic programs, highlighting an underappreciated role of ovarian microenvironments in orchestrating germ cell fates. Overall, our work provides insight into the spatial characteristics of early oogenesis and the regulatory role of ovarian microenvironments in germ cell fate within a spatial context.
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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